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Elements of a Paracrine Tubular Renin-Angiotensin System Along the Entire Nephron

Hypertension (Dallas, Tex. 1979), 1999-12, Vol.34 (6), p.1265-1265

1999

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Renin and kallikrein in connecting tubule of mouse

Kidney international, 2003-12, Vol.64 (6), p.2155-2162

2003

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Haplotypes of Angiotensinogen in Essential Hypertension

American journal of human genetics, 1997-06, Vol.60 (6), p.1448-1460

1997

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Molecular basis of human hypertension: Role of angiotensinogen

Cell, 1992-10, Vol.71 (1), p.169-180

1992

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A molecular variant of angiotensinogen associated with preeclampsia

Nature genetics, 1993-05, Vol.4 (1), p.59-61

1993

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Expression of angiotensinogen in proximal tubule as a function of glomerular filtration rate

Kidney international, 2004-06, Vol.65 (6), p.2153-2160

2004

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Angiotensinogen Thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first-trimester decidua

American journal of obstetrics and gynecology, 1999, Vol.180 (1), p.95-102

1999

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Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

Journal of human genetics, 2002-12, Vol.47 (12), p.665-676

2002

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Angiotensinogen as a risk factor for essential hypertension in Japan

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1285-1287

1994

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Lipoprotein lipase. Molecular model based on the pancreatic lipase x-ray structure: consequences for heparin binding and catalysis

The Journal of biological chemistry, 1994-02, Vol.269 (6), p.4626-4633

1994

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Angiotensinogen as a risk factor for essential hypertension in Japan

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1285-1287

1994

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Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension

Nature genetics, 1992-04, Vol.1 (1), p.72-75

1992

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The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

Science (American Association for the Advancement of Science), 1987-12, Vol.238 (4832), p.1411-1413

1987

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Angiotensin-converting enzyme gene polymorphism is associated with myocardial infarction but not with development of coronary stenosis

Circulation (New York, N.Y.), 1995-04, Vol.91 (8), p.2120-2124

1995

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Genetic Analysis of an Inherited Predisposition to Colon Cancer in a Family with a Variable Number of Adenomatous Polyps

The New England journal of medicine, 1990-03, Vol.322 (13), p.904-908

1990

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Direct detection and automated sequencing of individual alleles after electrophoretic strand separation : identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

Nucleic acids research, 1990-09, Vol.18 (18), p.5407-5411

1990

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Development of genetic hypotheses in essential hypertension

Journal of human genetics, 2001-01, Vol.46 (6), p.299-306

2001

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Easy calculations of lod scores and genetic risks on small computers

American journal of human genetics, 1984-03, Vol.36 (2), p.460-465

1984

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

American journal of human genetics, 1985-05, Vol.37 (3), p.482-498

1985

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Strategies for Multilocus Linkage Analysis in Humans

Proceedings of the National Academy of Sciences - PNAS, 1984-06, Vol.81 (11), p.3443-3446

1984

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Gene for Von Recklinghausen Neurofibromatosis is in the Pericentromeric Region of Chromosome 17

Science (American Association for the Advancement of Science), 1987-05, Vol.236 (4805), p.1100-1102

1987

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Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation

The Journal of clinical investigation, 1990-09, Vol.86 (3), p.735-750

1990

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Power and replication in case-control studies

American Journal of Hypertension, 2002-02, Vol.15 (2), p.201-205

2002

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A closely linked genetic marker for cystic fibrosis

Nature (London), 1985-01, Vol.318 (6044), p.382-384

1985

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Benign familial neonatal convulsions linked to genetic markers on chromosome 20

Nature (London), 1989-02, Vol.337 (6208), p.647-648

1989

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Elements of a Paracrine Tubular Renin-Angiotensin System Along the Entire Nephron

Renin and kallikrein in connecting tubule of mouse

Haplotypes of Angiotensinogen in Essential Hypertension

Molecular basis of human hypertension: Role of angiotensinogen

A molecular variant of angiotensinogen associated with preeclampsia

Expression of angiotensinogen in proximal tubule as a function of glomerular filtration rate

Angiotensinogen Thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first-trimester decidua

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript

Angiotensinogen as a risk factor for essential hypertension in Japan

Lipoprotein lipase. Molecular model based on the pancreatic lipase x-ray structure: consequences for heparin binding and catalysis

Angiotensinogen as a risk factor for essential hypertension in Japan

Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension

The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

Angiotensin-converting enzyme gene polymorphism is associated with myocardial infarction but not with development of coronary stenosis

Genetic Analysis of an Inherited Predisposition to Colon Cancer in a Family with a Variable Number of Adenomatous Polyps

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation : identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

Development of genetic hypotheses in essential hypertension

Easy calculations of lod scores and genetic risks on small computers

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

Strategies for Multilocus Linkage Analysis in Humans

Gene for Von Recklinghausen Neurofibromatosis is in the Pericentromeric Region of Chromosome 17

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation

Power and replication in case-control studies

A closely linked genetic marker for cystic fibrosis

Benign familial neonatal convulsions linked to genetic markers on chromosome 20

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